|
SMARCC2
(HGNC:11105)
|
Coffin-Siris syndrome
(MONDO_0015452)
|
Strong
|
|
|
SLC35A1
(HGNC:11021)
|
congenital disorder of glycosylation
(MONDO_0015286)
|
Moderate
|
|
|
SLC8A2
(HGNC:11069)
|
gastric cancer
(MONDO_0001056)
|
Limited
|
|
|
SLC30A3
(HGNC:11014)
|
schizophrenia
(MONDO_0005090)
|
Limited
|
|
|
SLC32A1
(HGNC:11018)
|
generalized epilepsy with febrile seizures plus
(MONDO_0018214)
|
Moderate
|
|
|
SLC2A5
(HGNC:11010)
|
hereditary fructose intolerance
(MONDO_0009249)
|
Refuted
|
|
|
SLC24A1
(HGNC:10975)
|
congenital stationary night blindness
(MONDO_0016293)
|
Moderate
|
|
|
SLC12A7
(HGNC:10915)
|
congenital hydrocephalus
(MONDO_0016349)
|
Limited
|
|
|
SLC25A10
(HGNC:10980)
|
mitochondrial DNA depletion syndrome
(MONDO_0018158)
|
Limited
|
|
|
CCL1
(HGNC:10609)
|
chronic obstructive pulmonary disease
(MONDO_0005002)
|
Limited
|
|
|
ST3GAL5
(HGNC:10872)
|
GM3 synthase deficiency
(MONDO_0018274)
|
Strong
|
|
|
SHOX2
(HGNC:10854)
|
atrial fibrillation
(MONDO_0004981)
|
Moderate
|
|
|
SKP1
(HGNC:10899)
|
breast cancer
(MONDO_0007254)
|
Limited
|
|
|
SI
(HGNC:10856)
|
congenital sucrase-isomaltase deficiency
(MONDO_0009114)
|
Moderate
|
|
|
SRSF5
(HGNC:10787)
|
bipolar disorder
(MONDO_0004985)
|
Limited
|
|
|
SHMT2
(HGNC:10852)
|
neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities
(MONDO_0030866)
|
Moderate
|
|
|
SETMAR
(HGNC:10762)
|
acute myeloid leukemia
(MONDO_0018874)
|
Limited
|
|
|
SF3B2
(HGNC:10769)
|
craniofacial microsomia
(MONDO_0015397)
|
Strong
|
|
|
CCL19
(HGNC:10617)
|
tuberculosis
(MONDO_0018076)
|
Limited
|
|
|
SF3A1
(HGNC:10765)
|
colorectal cancer
(MONDO_0005575)
|
Disputed
|
|